510(k) Report

FDA applicant

Chimera Research & Chemical, Inc.

Seminole, FL7 decisions1994–19970 recalls

FDA records 7 decisions for Chimera Research & Chemical, Inc. (Seminole, FL) from 1994 to 1997: 7 510(k) clearances. Most are in product codes KQO (Automated Urinalysis System) and CGX (Alkaline Picrate, Colorimetry, Creatinine). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Chimera Research & Chemical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chimera Research & Chemical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Chimera Research & Chemical, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Chimera Research & Chemical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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